Canonical Allele Identifier: CA2657843913
Gene: ODC1 HGNC NCBI

Linked Data

gnomAD v4: 2-10447922-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.10447922C>T , CM000664.2:g.10447922C>T GRCh38
NC_000002.11:g.10588048C>T , CM000664.1:g.10588048C>T GRCh37
NC_000002.10:g.10505499C>T NCBI36
NG_012105.1:g.5406G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000443218.2:c.-422G>A ENSP00000390691.2:n.-422G>A
ENST00000446285.6:c.-128+199G>A ENSP00000514632.1:n.-128+199G>A
ENST00000699835.1:c.-866G>A ENSP00000514633.1:n.-866G>A
ENST00000699836.1:c.-18+199G>A ENSP00000514634.1:n.-18+199G>A
ENST00000234111.9:c.-128+199G>A MANE Select ENSP00000234111.4:n.-128+199G>A
ENST00000234111.8:c.-128+199G>A ENSP00000234111.4:n.-128+199G>A
ENST00000446285.5:n.189+199G>A
NM_001287188.1:c.-415+199G>A NP_001274117.1:n.-415+199G>A
NM_002539.2:c.-128+199G>A NP_002530.1:n.-128+199G>A
NM_002539.3:c.-128+199G>A MANE Select NP_002530.1:n.-128+199G>A
NM_001287188.2:c.-415+199G>A NP_001274117.1:n.-415+199G>A
NM_001287189.2:c.-576G>A NP_001274118.1:n.-576G>A
NM_001287190.2:c.-422G>A NP_001274119.1:n.-422G>A
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